← Back to catalogue

Cable, Isolated, USB to RJ45

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1127403

by Respironics Inc.

Identity

Trade Name
Cable, Isolated, USB to RJ45 EUDAMED
Trilogy Evo FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Trilogy Evo Family Class I EUDAMED
Cable, Isolated, USB to RJ45 FDA UDI
Model / Reference
1127403 EUDAMED
Cable, Isolated, USB to RJ45 FDA UDI
Description
Cable, Isolated, USB to RJ45 FDA UDI

Identifiers

Catalog Number
1127403 FDA UDI
Primary DI / UDI-DI
00606959047624 EUDAMEDFDA UDI
Basic UDI-DI
0606959BM126LT EUDAMED
Direct Marketing DI
00606959047624 EUDAMED
FDA Product Code
NOU FDA UDI
CBK FDA UDI
EMDN Code
Z1203019080,Z1203019099 EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Cable, Isolated, USB to RJ45 by Respironics, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Respironics Inc.
EUDAMED SRN
US-MF-000002301
Authorised Representative
Philips Medical Systems Nederland B.V. NL-AR-000001422

Sources (2)

  • EUDAMED 293e6109-ebf2-42ed-93ea-2c1b4fa23c4e 61 fields · synced Jun 18, 2026
  • FDA UDI 03b1005b-05ce-476b-99a6-8ffda7f6a102 36 fields · synced May 30, 2026